Job Title: Clinical Research Associate - Bangalore, Chennai & Delhi
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Vacancy details
Vacancy description:
Job Code:
v-35
Job Title:
Clinical Research Associate - Bangalore, Chennai & Delhi
Job Category:
Clinical Research
Contract:
Permanent
Discipline:
CRA
Country:
India
Location:
Any Location
Min experience:
3 years
Annual salary:
Negotiable
Apply by:
05 Oct 2010
"At ICON, it's the people that set us Apart"
ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies
ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.
Job Title: Clinical Research Associate
Department: Clinical Operations
Location: Bangalore, Chennai & Delhi
Role Responsibility
Working within a highly qualified team you will identify, select, initiate and close-out investigational sites for clinical studies in phases II – IV ensuring that applicable regulations and principles of ICG-GCP are adhered to
Additional Responsibilities:
•Working independently and proactively to coordinate all necessary activities required to set up and monitor a study, completing accurate study status reports and maintaining study documentation
•Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested
•Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required
•Managing sponsor generated queries efficiently and responsible for study cost effectiveness
•Dependent on level of experience you may assist in training and mentoring less experienced CRA’s and/or manage CRA’s working on international projects
Experience and Qualification
With a University degree in medicine, science, or equivalent, you will have previous monitoring experience in medium sized studies including study start up and close out (for all roles above Entry Level). In addition, you will also require:
•You will have knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
•Fluent in English as well as the local language
•Excellent communication and interpersonal skills, both written and verbal enabling you to deal with queries in a timely manner
•Ability to produce accurate work to tight deadlines within a pressurised environment
•Computer literate with Microsoft Office
•Must be available to travel international and domestic at least 60% fly and drive and should possess a valid driving licence.
You will have the opportunity to progress your career and may wish to move into Project Management or into other related areas where you can further develop your skill set.
Come to ICON and be an important part of a well respected and growing company that believes the details of your career are every bit as critical as the work you do. You'll enjoy highly competitive compensation and an exceptional benefits package
ICON Clinical Research is an Equal Opportunity Employer committed to strength in diversity.
You must be logged in to apply for this position. Log in using the form on the right, at the top of the page beneath the logo, or click here to register.
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